Work

Delineation of the 9q31 deletion syndrome: Genomic microarray characterization of two patients with overlapping deletions

Year: 2018

Type: article

Study design: Case Report

Source: American Journal of Medical Genetics Part A

DOI: 10.1002/ajmg.a.40664

Authors: Sarah L. Dugan, Emanuele Panza, Amanda Openshaw, Lorenzo D. Botto, Jose A. Camacho, Reha M. Toydemir

Institutions: University of Utah, University of Bologna, ARUP Laboratories (United States), Miller Children's & Women's Hospital

Language: English

Topic: Genomic variations and chromosomal abnormalities

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funder: Wellcome Trust

OpenAlex ID: W2896779123

FWCI: 0.153

Cites: 17

Cited by: 4

Related to: 10